Canonical Allele Identifier: CA2269946080

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63488953C= , CM000679.2:g.63488953C=	GRCh38
NC_000017.10:g.61566314C= , CM000679.1:g.61566314C=	GRCh37
NC_000017.9:g.58920046C=	NCBI36
NG_011648.1:g.16881C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.2462C= MANE Select	ENSP00000290866.4:p.Ala821=
ENST00000290863.10:c.740C=	ENSP00000290863.6:p.Ala247=
ENST00000290866.9:c.2462C=	ENSP00000290866.4:p.Ala821=
ENST00000413513.7:c.740C=	ENSP00000392247.3:p.Ala247=
ENST00000428043.5:c.2462C=	ENSP00000397593.2:p.Ala821=
ENST00000577647.2:c.740C=	ENSP00000464149.1:p.Ala247=
ENST00000578839.5:c.*519+162C=	ENSP00000462110.2:n.*519+162C=
ENST00000579204.1:c.721C=	ENSP00000464629.1:n.721C=
ENST00000579314.5:c.*191C=	ENSP00000462599.1:n.*191C=
ENST00000582005.5:c.*382C=	ENSP00000462002.1:n.*382C=
ENST00000582761.1:c.230C=	ENSP00000462909.1:p.Ala77=
ENST00000584865.5:n.408C=
NM_000789.3:c.2462C=	NP_000780.1:p.Ala821=
NM_001178057.1:c.740C=	NP_001171528.1:p.Ala247=
NM_152830.2:c.740C=	NP_690043.1:p.Ala247=
XM_005257110.1:c.1913C=	XP_005257167.1:p.Ala638=
XM_006721737.2:c.800C=	XP_006721800.2:p.Ala267=
XM_006721737.3:c.800C=	XP_006721800.2:p.Ala267=
NM_000789.4:c.2462C= MANE Select	NP_000780.1:p.Ala821=
NM_001178057.2:c.740C=	NP_001171528.1:p.Ala247=
NM_152830.3:c.740C=	NP_690043.1:p.Ala247=
NM_001382700.1:c.1895C=	NP_001369629.1:p.Ala632=
NM_001382701.1:c.1610C=	NP_001369630.1:p.Ala537=
NM_001382702.1:c.379+162C=	NP_001369631.1:n.379+162C=
NR_168483.1:n.840C=